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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547721Generated: October 28, 2026

2-Vinylpyridine → HCID 67199350, compound

https://huagongshe.com/reaction/547721

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-VinylpyridineHCID 7521—
ReactantTriethylamineHCID 8471—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant3-Bromo-1-phenyl-5-(pyridin-2-yl)-1,2-dihydropyridin-2-oneHCID 22319065—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 67199350HCID 671993508.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

23 mg of 3-bromo-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-one was dissolved in 20 ml of acetonitrile. To the mixture were added 0.2 mg of palladium acetate, 4.3 mg of tri-o-tolylphosphine and 0.04 ml of triethylamine, followed by stirring at 110° C. in nitrogen atmosphere overnight. To the mixture was added 9.2 mg of 2-vinylpyridine, followed by stirring at 110° C. in nitrogen atmosphere for 5 hours. After cooling to room temperature, the reaction mixture was poured into water, followed by extracting with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel chromatography (hexane/ethyl acetate system), to give 2 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939549B2
Source datasetuspto-grants-2011_05
ORD IDord-4408c712c04f49c2af114f3346d854ff
Source noteuspto-grants-2011_05